Clinical effects of Sevoflurane
Due to the preferable pharmacodynamics, Sevoflurane is the most favoured drug for the induction and maintenance of anaesthesia. Its low blood-gas partition coefficient helps to rapid alteration of the level of anaesthesia.
CVS effects:
→ Mild ↓ cardiac contractility (dose-dependent, equal to isoflurane)
→ Mild ↓ SVR (dose-dependent, equal to Halothane)
→ Mild ↓ BP (dose-dependent, most least compared to others)
→ Minimal effect on HR
→ May cause prolongation of the QT interval
→ Not associated with coronary steal
→ Doesn't sensitize the myocardium
→ No effect on splanchnic blood flow
Respiratory effects:
→ Non-irritant
→ Dose-dependent Tidal volume depression (less than Isoflurane, equal to Halothane)
→ ↑ RR (equal to Isoflurane, more than Halothane)
→ ↓ MV causing ↑ PaCO2
→ Depression of hypoxic and hypercapnic ventilatory drive
→ Inhibition of hypoxic pulmonary vasoconstriction
→ Bronchial smooth muscle relaxation and reversal of bronchospasm
CNS effects:
→ Effect on cerebral autoregulation is less pronounced than Isoflurane
→ > 1.5 MAC may impair cerebral autoregulation
→ Minimal effect on ICP at 0.5 - 1.0 MAC due to preservation of autoregulation
→ Slight in CBF in normocarbia
→ No excitatory effect on EEG
→ Potentiate neuromuscular blocking drugs
→ Compared to Halothane, higher incidence of postoperative agitation and delirium in children
Neuromuscular:
→ Dose-dependent muscle relaxation
→ Can produce adequate relaxation for intubation
Hepatic:
→ Maintain total hepatic blood flow
→ No immune-mediated hepatic toxicity
Renal:
→ Barium hydroxide and Sodalime may degrade Sevoflurane and may produce compound A
→ No proven renal toxicity
→ Preserve renal blood flow
Others:
→ Causes uterine relaxation
→ PONV
Reference -
Pharmacology Of Inhalational Anaesthetic Agents – Part 2
Pharmacology for anaesthesia and intensive care, 4th edition
Smith and Aitkenhead's Textbook of Anaesthesia, 7th edition
Morgan and Mikhail's Clinical anesthesiology, 6th edition
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